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Long-term growth hormone responses to nonspecific hypothalamic hormones in acromegalic patients.

Abstract
Nonspecific hypothalamic hormones such as thyrotropin-releasing hormone or luteinizing hormone-releasing hormone, or both, elicited abnormal growth hormone responses in 73 of 108 (67.6%) acromegalic patients. After transsphenoidal adenomectomy, the provocative tests using these hormones were repeated in 26 patients with abnormal preoperative growth hormone responses to study variations in these responses during a 1-8-year observation period (average duration, 4 years). After surgery, 7 of the 26 patients regained normal basal growth hormone levels (less than 5 ng/mL) and manifested normal responses to the hypothalamic hormones. During the postoperative observation period, their basal growth hormone levels remained normal as did their responses to provocation with hypothalamic hormones, confirming that the adenoma had been completely resected. Eight other patients demonstrated normal growth hormone levels after surgery; however, they continued to have abnormal responses to provocation with hypothalamic hormones, suggesting the presence of residual adenomatous tissue in the gland. These patients manifested no marked increase in basal or peak growth hormone levels during the follow-up period (from less than 1 to less than 7.5 years) and they were all in clinical remission without any other treatment. Only one incompletely adenomectomized patient who had received no additional treatment experienced regrowth of the tumor. The main factor affecting the surgical results appears to be the preoperative basal growth hormone level, because abnormal growth hormone secretion ceased in all patients who had manifested preoperative levels below 45 ng/mL. Technical refinements of the operative procedure are another important factor in the postoperative outcome. Peritumoral tissue resection after simple selective adenomectomy is mandatory for better surgical results. Our studies indicate that fairly good results can be obtained without risk of the recurrence of the tumor or regrowth, when postoperative growth hormone levels are below 5 ng/mL and that the results are not affected by the postoperative growth hormone responses to provocation with hypothalamic hormones.
AuthorsM Watanabe, A Kuwayama, T Nakane, N Kanie, T Kato, T Takahashi, N Kageyama
JournalSurgical neurology (Surg Neurol) Vol. 24 Issue 4 Pg. 449-56 (Oct 1985) ISSN: 0090-3019 [Print] United States
PMID4035555 (Publication Type: Journal Article)
Chemical References
  • Hypothalamic Hormones
  • Growth Hormone
Topics
  • Acromegaly (drug therapy, surgery)
  • Adenoma (surgery)
  • Adolescent
  • Adult
  • Aged
  • Child
  • Female
  • Growth Hormone (blood)
  • Humans
  • Hypothalamic Hormones (therapeutic use)
  • Male
  • Middle Aged
  • Pituitary Neoplasms (surgery)
  • Time Factors

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